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Senior Manufacturing Associate I / II
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Full-time
- The Senior Manufacturing Associate I/II is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products.
- The Senior Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and/or Good Laboratory Practices (GLP).
- As needed, the Senior Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write Corrective and Preventive Actions (CAPAs); and specify, commission, and qualify new equipment.
- The Senior Manufacturing Associate will responsible for upstream unit operations (see expansion, bioreactor operations, cell culture harvest).
- The Senior Manfuacturing Associate will have past experience and working knowledge of upstream processing equipment (incubators, biosafety cabinets, bioreactors, cell counters, blood gas analyzers, metabolite testing equipment).
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